Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37700 | A02 | 32241766 | G | A | missense_variant | MODERATE | c.1007C>T|p.Thr336Ile |
S156 |
2 | BAA02g37700 | A02 | 32242699 | C | T | missense_variant&splice_region_variant | MODERATE | c.569G>A|p.Gly190Glu |
S124 |
3 | BAA02g37700 | A02 | 32242986 | C | T | missense_variant | MODERATE | c.463G>A|p.Asp155Asn |
S189 |
4 | BAA02g37700 | A02 | 32243995 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Leu |
S109 |
5 | BAA02g37700 | A02 | 32245073 | C | T | upstream_gene_variant | MODIFIER | c.-996G>A| |
S140 |
6 | BAA02g37700 | A02 | 32245426 | C | T | upstream_gene_variant | MODIFIER | c.-1349G>A| |
S48 |
7 | BAA02g37700 | A02 | 32246355 | G | A | upstream_gene_variant | MODIFIER | c.-2278C>T| |
S69 |
8 | BAA02g37700 | A02 | 32246565 | G | A | upstream_gene_variant | MODIFIER | c.-2488C>T| |
S150 |
9 | BAA02g37700 | A02 | 32246666 | C | T | upstream_gene_variant | MODIFIER | c.-2589G>A| |
S100 |
10 | BAA02g37700 | A02 | 32246761 | A | G | upstream_gene_variant | MODIFIER | c.-2684T>C| |
S267 |
11 | BAA02g37700 | A02 | 32247503 | G | A | upstream_gene_variant | MODIFIER | c.-3426C>T| |
S245 |
12 | BAA02g37700 | A02 | 32247721 | G | A | upstream_gene_variant | MODIFIER | c.-3644C>T| |
S230 |
13 | BAA02g37700 | A02 | 32248841 | G | A | upstream_gene_variant | MODIFIER | c.-4764C>T| |
S168 |